Duns Number:482489007
Device Description: Bottle Spike Type A
Catalog Number
-
Brand Name
Bottle Spike Type A
Version/Model Number
640458
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K151048,K151048,K151048
Product Code
IZQ
Product Code Name
Injector, Contrast Medium, Automatic
Public Device Record Key
b9b3863c-f47a-47bd-bf76-57fe7671e012
Public Version Date
May 14, 2020
Public Version Number
1
DI Record Publish Date
May 06, 2020
Package DI Number
37630039301492
Quantity per Package
60
Contains DI Package
17630039301498
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 84 |